Department of Medical, Surgical, Neurological, Metabolic and Aging Sciences, University of Campania "Luigi Vanvitelli", Napoli, Italy.
MRI Research Center SUN-FISM, University of Campania "Luigi Vanvitelli", Napoli, Italy.
Mov Disord. 2017 Dec;32(12):1710-1719. doi: 10.1002/mds.27139. Epub 2017 Sep 26.
Impulse control disorders can be triggered by dopamine replacement therapies in patients with PD. Using resting-state functional MRI, we investigated the intrinsic brain network connectivity at baseline in a cohort of drug-naive PD patients who successively developed impulse control disorders over a 36-month follow-up period compared with patients who did not.
Baseline 3-Tesla MRI images of 30 drug-naive PD patients and 20 matched healthy controls were analyzed. The impulse control disorders' presence and severity at follow-up were assessed by the Questionnaire for Impulsive-Compulsive Disorders in Parkinson's Disease Rating Scale. Single-subject and group-level independent component analysis was used to investigate functional connectivity differences within the major resting-state networks. We also compared internetwork connectivity between patients. Finally, a multivariate Cox regression model was used to investigate baseline predictors of impulse control disorder development.
At baseline, decreased connectivity in the default-mode and right central executive networks and increased connectivity in the salience network were detected in PD patients with impulse control disorders at follow-up compared with those without. Increased default-mode/central executive internetwork connectivity was significantly associated with impulse control disorders development (P < 0.05).
Our findings demonstrated that abnormal brain connectivity in the three large-scale networks characterizes drug-naive PD patients who will eventually develop impulse control disorders while on dopaminergic treatment. We hypothesize that these divergent cognitive and limbic network connectivity changes could represent a potential biomarker and an additional risk factor for the emergence of impulse control disorders. © 2017 International Parkinson and Movement Disorder Society.
冲动控制障碍可由多巴胺替代疗法在 PD 患者中引发。我们使用静息态功能磁共振成像,在一组连续接受 36 个月随访的药物初治 PD 患者中,与未发生冲动控制障碍的患者相比,在基线时研究了药物初治 PD 患者冲动控制障碍的固有脑网络连接。
分析了 30 名药物初治 PD 患者和 20 名匹配的健康对照者的基线 3-Tesla MRI 图像。通过帕金森病冲动-强迫障碍评定量表(Questionnaire for Impulsive-Compulsive Disorders in Parkinson's Disease Rating Scale)评估随访时冲动控制障碍的存在和严重程度。采用单个体和组水平独立成分分析方法,研究主要静息态网络内的功能连接差异。我们还比较了患者之间的网络间连接。最后,采用多元 Cox 回归模型,研究基线时冲动控制障碍发生的预测因素。
与无冲动控制障碍的患者相比,在基线时,随访时出现冲动控制障碍的 PD 患者默认模式和右侧中央执行网络的连接减少,突显网络的连接增加。默认模式/中央执行网络间连接的增加与冲动控制障碍的发展显著相关(P < 0.05)。
我们的研究结果表明,在接受多巴胺能治疗的药物初治 PD 患者中,三个大网络的异常脑连接特征是最终会发展为冲动控制障碍的患者。我们假设,这些认知和边缘网络连接变化的差异可能代表了冲动控制障碍出现的潜在生物标志物和附加风险因素。